[English] 日本語
Yorodumi- PDB-7ey2: Bifunctional xylosidase/glucosidase LXYL D300N mutant with interm... -
+
Open data
-
Basic information
| Entry | Database: PDB / ID: 7ey2 | ||||||
|---|---|---|---|---|---|---|---|
| Title | Bifunctional xylosidase/glucosidase LXYL D300N mutant with intermediate substrate xylose | ||||||
Components | Beta-D-xylosidase/beta-D-glucosidase | ||||||
Keywords | HYDROLASE / glycoside hydrolases / xylosidases / bifunctional | ||||||
| Function / homology | Function and homology informationglucan catabolic process / beta-glucosidase / beta-glucosidase activity / extracellular region Similarity search - Function | ||||||
| Biological species | Lentinula edodes (shiitake mushroom) | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.43 Å | ||||||
Authors | Gong, W.M. / Yang, L.Y. | ||||||
| Funding support | China, 1items
| ||||||
Citation | Journal: To Be PublishedTitle: Bifunctional xylosidase/glucosidase LXYL with intermediate substrate xylose Authors: Gong, W.M. / Yang, L.Y. | ||||||
| History |
|
-
Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
|---|
-
Downloads & links
-
Download
| PDBx/mmCIF format | 7ey2.cif.gz | 893.5 KB | Display | PDBx/mmCIF format |
|---|---|---|---|---|
| PDB format | pdb7ey2.ent.gz | 745.7 KB | Display | PDB format |
| PDBx/mmJSON format | 7ey2.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 7ey2_validation.pdf.gz | 7.6 MB | Display | wwPDB validaton report |
|---|---|---|---|---|
| Full document | 7ey2_full_validation.pdf.gz | 7.8 MB | Display | |
| Data in XML | 7ey2_validation.xml.gz | 175.1 KB | Display | |
| Data in CIF | 7ey2_validation.cif.gz | 243.2 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ey/7ey2 ftp://data.pdbj.org/pub/pdb/validation_reports/ey/7ey2 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7ey1C ![]() 7yo6C ![]() 7yo7C ![]() 8gyyC ![]() 6kj0S S: Starting model for refinement C: citing same article ( |
|---|---|
| Similar structure data | Similarity search - Function & homology F&H Search |
-
Links
-
Assembly
| Deposited unit | ![]()
| ||||||||
|---|---|---|---|---|---|---|---|---|---|
| 1 | ![]()
| ||||||||
| 2 | ![]()
| ||||||||
| 3 | ![]()
| ||||||||
| Unit cell |
|
-
Components
-Protein / Non-polymers , 2 types, 1307 molecules ABCDEF

| #12: Water | ChemComp-HOH / |
|---|---|
| #1: Protein | Mass: 86312.070 Da / Num. of mol.: 6 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Lentinula edodes (shiitake mushroom) / Gene: Lxyl-p1-2 / Production host: ![]() |
-Sugars , 10 types, 46 molecules 






| #2: Polysaccharide | beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta- ...beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose Source method: isolated from a genetically manipulated source #3: Polysaccharide | alpha-D-mannopyranose-(1-2)-beta-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-3)-alpha-D- ...alpha-D-mannopyranose-(1-2)-beta-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-3)-alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose Source method: isolated from a genetically manipulated source #4: Polysaccharide | Source method: isolated from a genetically manipulated source #5: Polysaccharide | alpha-D-mannopyranose-(1-2)-beta-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-3)-[alpha-D- ...alpha-D-mannopyranose-(1-2)-beta-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-6)]alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose | Type: oligosaccharide / Mass: 1397.245 Da / Num. of mol.: 1 / Source method: obtained synthetically #6: Polysaccharide | alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-alpha-D- ...alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-2)-alpha-D-mannopyranose-(1-3)-alpha-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose #7: Polysaccharide | alpha-D-mannopyranose-(1-2)-beta-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-3)-alpha-D- ...alpha-D-mannopyranose-(1-2)-beta-D-mannopyranose-(1-3)-[alpha-D-mannopyranose-(1-3)-alpha-D-mannopyranose-(1-6)]beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose | Type: oligosaccharide / Mass: 1031.912 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source #8: Sugar | ChemComp-NAG / #9: Sugar | #10: Sugar | ChemComp-BMA / | #11: Sugar | |
|---|
-Details
| Has ligand of interest | Y |
|---|---|
| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
|---|
-
Sample preparation
| Crystal | Density Matthews: 3.14 Å3/Da / Density % sol: 60.79 % |
|---|---|
| Crystal grow | Temperature: 289.15 K / Method: vapor diffusion, hanging drop / Details: 20% PEG 3350, 0.1M Hepes pH 5.0, 0.2% MgCl2 |
-Data collection
| Diffraction | Mean temperature: 100 K / Serial crystal experiment: N |
|---|---|
| Diffraction source | Source: SYNCHROTRON / Site: SSRF / Beamline: BL17U / Wavelength: 0.979 Å |
| Detector | Type: ADSC QUANTUM 315r / Detector: CCD / Date: Aug 8, 2016 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.979 Å / Relative weight: 1 |
| Reflection | Resolution: 2.43→160.12 Å / Num. obs: 227425 / % possible obs: 98.8 % / Redundancy: 4.8 % / Rmerge(I) obs: 0.114 / Net I/σ(I): 36.3 |
| Reflection shell | Resolution: 2.43→2.47 Å / Rmerge(I) obs: 0.532 / Num. unique obs: 11317 |
-
Processing
| Software |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 6KJ0 Resolution: 2.43→160.12 Å / Cor.coef. Fo:Fc: 0.948 / Cor.coef. Fo:Fc free: 0.917 / SU B: 6.989 / SU ML: 0.16 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R: 0.322 / ESU R Free: 0.233 / Stereochemistry target values: MAXIMUM LIKELIHOOD Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS U VALUES : REFINED INDIVIDUALLY
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso max: 107.61 Å2 / Biso mean: 30.324 Å2 / Biso min: 14.95 Å2
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: final / Resolution: 2.43→160.12 Å
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refine LS restraints |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| LS refinement shell | Resolution: 2.432→2.495 Å / Rfactor Rfree error: 0 / Total num. of bins used: 20
|
Movie
Controller
About Yorodumi



Lentinula edodes (shiitake mushroom)
X-RAY DIFFRACTION
China, 1items
Citation




PDBj




